Canonical Allele Identifier: CA2789814139

Gene: OAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124398243_124398244insAGTT , CM000672.2:g.124398243_124398244insAGTT	GRCh38
NC_000010.10:g.126086812_126086813insAGTT , CM000672.1:g.126086812_126086813insAGTT	GRCh37
NC_000010.9:g.126076802_126076803insAGTT	NCBI36
NG_008861.1:g.25707_25708insAACT , LRG_685:g.25707_25708insAACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368845.6:c.1160-142_1160-141insAACT MANE Select	ENSP00000357838.5:n.1160-142_1160-141insAACT
ENST00000368845.5:c.1160-142_1160-141insAACT	ENSP00000357838.5:n.1160-142_1160-141insAACT
ENST00000471127.1:n.670-142_670-141insAACT
ENST00000539214.5:c.746-142_746-141insAACT	ENSP00000439042.1:n.746-142_746-141insAACT
NM_000274.3:c.1160-142_1160-141insAACT , LRG_685t1:c.1160-142_1160-141insAACT	NP_000265.1:n.1160-142_1160-141insAACT
NM_001171814.1:c.746-142_746-141insAACT	NP_001165285.1:n.746-142_746-141insAACT
XM_006717871.2:c.1160-142_1160-141insAACT	XP_006717934.1:n.1160-142_1160-141insAACT
XM_011539833.1:c.1160-142_1160-141insAACT	XP_011538135.1:n.1160-142_1160-141insAACT
XM_011539834.1:c.1160-142_1160-141insAACT	XP_011538136.1:n.1160-142_1160-141insAACT
NM_001322965.1:c.1160-142_1160-141insAACT	NP_001309894.1:n.1160-142_1160-141insAACT
NM_001322966.1:c.1160-142_1160-141insAACT	NP_001309895.1:n.1160-142_1160-141insAACT
NM_001322967.1:c.1160-142_1160-141insAACT	NP_001309896.1:n.1160-142_1160-141insAACT
NM_001322968.1:c.1160-142_1160-141insAACT	NP_001309897.1:n.1160-142_1160-141insAACT
NM_001322969.1:c.1160-142_1160-141insAACT	NP_001309898.1:n.1160-142_1160-141insAACT
NM_001322970.1:c.1160-142_1160-141insAACT	NP_001309899.1:n.1160-142_1160-141insAACT
NM_001322971.1:c.839-142_839-141insAACT	NP_001309900.1:n.839-142_839-141insAACT
NM_001322974.1:c.560-142_560-141insAACT	NP_001309903.1:n.560-142_560-141insAACT
XM_017016279.1:c.560-142_560-141insAACT	XP_016871768.1:n.560-142_560-141insAACT
NM_000274.4:c.1160-142_1160-141insAACT MANE Select	NP_000265.1:n.1160-142_1160-141insAACT
NM_001322965.2:c.1160-142_1160-141insAACT	NP_001309894.1:n.1160-142_1160-141insAACT
NM_001322966.2:c.1160-142_1160-141insAACT	NP_001309895.1:n.1160-142_1160-141insAACT
NM_001322967.2:c.1160-142_1160-141insAACT	NP_001309896.1:n.1160-142_1160-141insAACT
NM_001322968.2:c.1160-142_1160-141insAACT	NP_001309897.1:n.1160-142_1160-141insAACT
NM_001322969.2:c.1160-142_1160-141insAACT	NP_001309898.1:n.1160-142_1160-141insAACT
NM_001322970.2:c.1160-142_1160-141insAACT	NP_001309899.1:n.1160-142_1160-141insAACT
NM_001322971.2:c.839-142_839-141insAACT	NP_001309900.1:n.839-142_839-141insAACT
NM_001322974.2:c.560-142_560-141insAACT	NP_001309903.1:n.560-142_560-141insAACT
NM_001171814.2:c.746-142_746-141insAACT	NP_001165285.1:n.746-142_746-141insAACT